PL188823B1 - Sól pirymetanilu i zawierająca ją kompozycja grzybobójcza - Google Patents

Sól pirymetanilu i zawierająca ją kompozycja grzybobójcza

Info

Publication number: PL188823B1
Authority: PL; Poland
Prior art keywords: pyrimethanil; acid; salt; saccharin; dipyrimethanil
Prior art date: 1996-04-27

Application number

PL97329475A

Other languages

English (en)

Polish (pl)

Other versions

PL329475A1 (en

Inventor

David Stock

Geoffrey Gower Briggs

Donald James Simpson

Original Assignee

Bayer Cropscience Ltd

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1996-04-27

Filing date

1997-04-25

Publication date

2005-04-29

1997-04-25 Application filed by Bayer Cropscience Ltd filed Critical Bayer Cropscience Ltd

1999-03-29 Publication of PL329475A1 publication Critical patent/PL329475A1/xx

2005-04-29 Publication of PL188823B1 publication Critical patent/PL188823B1/pl

Links

150000003839 salts Chemical class 0.000 title claims abstract description 15
230000000855 fungicidal effect Effects 0.000 title claims abstract description 7
ZLIBICFPKPWGIZ-UHFFFAOYSA-N pyrimethanil Chemical compound CC1=CC(C)=NC(NC=2C=CC=CC=2)=N1 ZLIBICFPKPWGIZ-UHFFFAOYSA-N 0.000 claims abstract description 94
239000005828 Pyrimethanil Substances 0.000 claims abstract description 82
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims abstract description 18
239000000203 mixture Substances 0.000 claims abstract description 17
229940081974 saccharin Drugs 0.000 claims abstract description 15
239000000901 saccharin and its Na,K and Ca salt Substances 0.000 claims abstract description 15
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 claims abstract description 14
CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical compound C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 claims abstract description 14
235000019204 saccharin Nutrition 0.000 claims abstract description 14
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims abstract description 12
239000002253 acid Substances 0.000 claims abstract description 12
XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 claims abstract description 12
WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 claims abstract description 9
LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 claims abstract description 9
QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 claims abstract description 9
239000005642 Oleic acid Substances 0.000 claims abstract description 9
ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 claims abstract description 9
QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 claims abstract description 9
LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims abstract description 6
ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 claims abstract description 6
150000004668 long chain fatty acids Chemical class 0.000 claims abstract description 6
150000007524 organic acids Chemical class 0.000 claims abstract description 6
239000003085 diluting agent Substances 0.000 claims abstract description 3
150000001875 compounds Chemical class 0.000 claims description 10
MIOPJNTWMNEORI-UHFFFAOYSA-N camphorsulfonic acid Chemical compound C1CC2(CS(O)(=O)=O)C(=O)CC1C2(C)C MIOPJNTWMNEORI-UHFFFAOYSA-N 0.000 claims description 6
239000004480 active ingredient Substances 0.000 claims description 5
229940049964 oleate Drugs 0.000 claims description 5
XNGIFLGASWRNHJ-UHFFFAOYSA-M phthalate(1-) Chemical compound OC(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-M 0.000 claims description 5
XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 claims description 5
BHHUJKQASFYDMY-UHFFFAOYSA-N 4,7-dimethoxy-1,1-dioxo-1,2-benzothiazol-3-one Chemical compound COC1=CC=C(OC)C2=C1C(=O)NS2(=O)=O BHHUJKQASFYDMY-UHFFFAOYSA-N 0.000 claims description 4
OFOBLEOULBTSOW-UHFFFAOYSA-L Malonate Chemical compound [O-]C(=O)CC([O-])=O OFOBLEOULBTSOW-UHFFFAOYSA-L 0.000 claims description 4
LCPDWSOZIOUXRV-UHFFFAOYSA-N phenoxyacetic acid Chemical compound OC(=O)COC1=CC=CC=C1 LCPDWSOZIOUXRV-UHFFFAOYSA-N 0.000 claims description 4
CMPQUABWPXYYSH-UHFFFAOYSA-N phenyl phosphate Chemical compound OP(O)(=O)OC1=CC=CC=C1 CMPQUABWPXYYSH-UHFFFAOYSA-N 0.000 claims description 4
CVHZOJJKTDOEJC-UHFFFAOYSA-M 1,1-dioxo-1,2-benzothiazol-3-olate Chemical compound C1=CC=C2C([O-])=NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-M 0.000 claims description 3
239000013543 active substance Substances 0.000 abstract 2
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
201000010099 disease Diseases 0.000 description 6
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 6
238000011084 recovery Methods 0.000 description 6
208000015181 infectious disease Diseases 0.000 description 5
241000196324 Embryophyta Species 0.000 description 4
POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 4
238000009472 formulation Methods 0.000 description 4
IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 4
239000000243 solution Substances 0.000 description 4
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
241000123650 Botrytis cinerea Species 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
241000233866 Fungi Species 0.000 description 2
239000005639 Lauric acid Substances 0.000 description 2
235000021314 Palmitic acid Nutrition 0.000 description 2
241000736122 Parastagonospora nodorum Species 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
230000000694 effects Effects 0.000 description 2
239000007788 liquid Substances 0.000 description 2
125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 2
239000000126 substance Substances 0.000 description 2
BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 2
MIOPJNTWMNEORI-GMSGAONNSA-N (S)-camphorsulfonic acid Chemical compound C1C[C@@]2(CS(O)(=O)=O)C(=O)C[C@@H]1C2(C)C MIOPJNTWMNEORI-GMSGAONNSA-N 0.000 description 1
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
241001480061 Blumeria graminis Species 0.000 description 1
241001465180 Botrytis Species 0.000 description 1
ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 1
241000221787 Erysiphe Species 0.000 description 1
231100000674 Phytotoxicity Toxicity 0.000 description 1
CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 1
241000209140 Triticum Species 0.000 description 1
241000317942 Venturia <ichneumonid wasp> Species 0.000 description 1
235000013339 cereals Nutrition 0.000 description 1
229940125904 compound 1 Drugs 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
239000000428 dust Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
230000002538 fungal effect Effects 0.000 description 1
239000000417 fungicide Substances 0.000 description 1
150000003949 imides Chemical class 0.000 description 1
238000005259 measurement Methods 0.000 description 1
238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
244000052769 pathogen Species 0.000 description 1
230000001717 pathogenic effect Effects 0.000 description 1
230000003032 phytopathogenic effect Effects 0.000 description 1
230000008635 plant growth Effects 0.000 description 1
230000005855 radiation Effects 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000011550 stock solution Substances 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
239000004563 wettable powder Substances 0.000 description 1

Classifications

- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/32—One oxygen, sulfur or nitrogen atom
- C07D239/42—One nitrogen atom
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/3804—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)] not used, see subgroups
- C07F9/3834—Aromatic acids (P-C aromatic linkage)

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Health & Medical Sciences (AREA)
General Health & Medical Sciences (AREA)
Dentistry (AREA)
Environmental Sciences (AREA)
Engineering & Computer Science (AREA)
Pest Control & Pesticides (AREA)
Agronomy & Crop Science (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Plant Pathology (AREA)
Biochemistry (AREA)
Molecular Biology (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

PL97329475A 1996-04-27 1997-04-25 Sól pirymetanilu i zawierająca ją kompozycja grzybobójcza PL188823B1 (pl)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
GBGB9608771.3A GB9608771D0 (en)	1996-04-27	1996-04-27	Pyrimethanil salts
PCT/GB1997/001141 WO1997040682A1 (en)	1996-04-27	1997-04-25	Fungicide salts

Publications (2)

Publication Number	Publication Date
PL329475A1 PL329475A1 (en)	1999-03-29
PL188823B1 true PL188823B1 (pl)	2005-04-29

Family

ID=10792764

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
PL97329475A PL188823B1 (pl)	1996-04-27	1997-04-25	Sól pirymetanilu i zawierająca ją kompozycja grzybobójcza

Country Status (16)

Country	Link
US (1)	US6030977A (de)
EP (1)	EP0900015B1 (de)
JP (1)	JP4142102B2 (de)
KR (1)	KR100430538B1 (de)
CN (1)	CN1121138C (de)
AT (1)	ATE222455T1 (de)
AU (1)	AU717759B2 (de)
BR (1)	BR9708832A (de)
CA (1)	CA2252958C (de)
DE (1)	DE69714840T2 (de)
ES (1)	ES2179327T3 (de)
GB (1)	GB9608771D0 (de)
HU (1)	HU228649B1 (de)
IL (1)	IL126459A (de)
PL (1)	PL188823B1 (de)
WO (1)	WO1997040682A1 (de)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
AU2002315388A1 (en) *	2001-06-21	2003-01-08	Ariad Pharmaceuticals, Inc.	Novel phenylamino-pyrimidines and uses thereof
FR2829669A1 (fr) *	2001-09-18	2003-03-21	Aventis Cropscience Sa	Composition fongicide comprenant un compose de la famille des anilinopyrimidines et de l'iprodione
CA2554236C (en)	2004-02-04	2012-09-11	Janssen Pharmaceutica N.V.	Synergistic antifungal didecyl dimethyl ammonium chloride compositions
GB0706044D0 (en) *	2007-03-28	2007-05-09	Syngenta Ltd	C0-Crystals
MX353308B (es)	2008-05-21	2018-01-08	Ariad Pharma Inc	Derivados fosforosos como inhibidores de cinasa.
US9273077B2 (en)	2008-05-21	2016-03-01	Ariad Pharmaceuticals, Inc.	Phosphorus derivatives as kinase inhibitors
EP2208623B1 (de)	2009-01-08	2014-11-19	Global Dynamix AG	Ventilvorrichtung, Fahrzeugreifendruckmesseinheit und Fahrzeugreifendrucksystem
GB201006326D0 (en) *	2010-04-15	2010-06-02	Syngenta Ltd	Formulation
EP2704572B1 (de)	2011-05-04	2015-12-30	Ariad Pharmaceuticals, Inc.	Verfahren zur hemmung der zellproliferation bei efgr-vermitteltem krebs
WO2013050663A1 (fr)	2011-10-04	2013-04-11	Xeda International	Nouvelles formulations de pyriméthanil et leurs utilisations dans le traitement des cultures
WO2013169401A1 (en)	2012-05-05	2013-11-14	Ariad Pharmaceuticals, Inc.	Compounds for inhibiting cell proliferation in egfr-driven cancers
WO2014053398A1 (en)	2012-10-01	2014-04-10	Basf Se	Pesticidal mixtures comprising jasmonic acid or a derivative thereof
US9611283B1 (en)	2013-04-10	2017-04-04	Ariad Pharmaceuticals, Inc.	Methods for inhibiting cell proliferation in ALK-driven cancers

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3639902A1 (de) *	1986-11-22	1988-06-01	Bayer Ag	Saccharin-salze von substituierten hydroxypropylaminen
US5366995A (en) *	1991-05-01	1994-11-22	Mycogen Corporation	Fatty acid based compositions for the control of established plant infections
JP3634409B2 (ja) *	1993-09-13	2005-03-30	ビーエーエスエフアクチェンゲゼルシャフト	殺菌剤混合物

1996
- 1996-04-27 GB GBGB9608771.3A patent/GB9608771D0/en active Pending
1997
- 1997-04-25 WO PCT/GB1997/001141 patent/WO1997040682A1/en not_active Ceased
- 1997-04-25 IL IL12645997A patent/IL126459A/xx not_active IP Right Cessation
- 1997-04-25 AU AU23983/97A patent/AU717759B2/en not_active Expired
- 1997-04-25 JP JP53866197A patent/JP4142102B2/ja not_active Expired - Lifetime
- 1997-04-25 US US09/171,865 patent/US6030977A/en not_active Expired - Lifetime
- 1997-04-25 DE DE69714840T patent/DE69714840T2/de not_active Expired - Lifetime
- 1997-04-25 ES ES97919549T patent/ES2179327T3/es not_active Expired - Lifetime
- 1997-04-25 AT AT97919549T patent/ATE222455T1/de not_active IP Right Cessation
- 1997-04-25 PL PL97329475A patent/PL188823B1/pl unknown
- 1997-04-25 CA CA002252958A patent/CA2252958C/en not_active Expired - Lifetime
- 1997-04-25 EP EP97919549A patent/EP0900015B1/de not_active Expired - Lifetime
- 1997-04-25 CN CN97195601A patent/CN1121138C/zh not_active Expired - Lifetime
- 1997-04-25 KR KR19980708586A patent/KR100430538B1/ko not_active Expired - Lifetime
- 1997-04-25 BR BR9708832A patent/BR9708832A/pt not_active IP Right Cessation
- 1997-04-25 HU HU9902741A patent/HU228649B1/hu unknown

Also Published As

Publication number	Publication date
JP4142102B2 (ja)	2008-08-27
PL329475A1 (en)	1999-03-29
DE69714840D1 (de)	2002-09-26
CN1121138C (zh)	2003-09-17
EP0900015A1 (de)	1999-03-10
WO1997040682A1 (en)	1997-11-06
DE69714840T2 (de)	2003-03-20
CA2252958A1 (en)	1997-11-06
IL126459A0 (en)	1999-10-28
HUP9902741A2 (hu)	1999-12-28
HUP9902741A3 (en)	2000-06-28
AU2398397A (en)	1997-11-19
BR9708832A (pt)	1999-08-03
EP0900015B1 (de)	2002-08-21
JP2000509065A (ja)	2000-07-18
KR20000065041A (ko)	2000-11-06
IL126459A (en)	2003-04-10
AU717759B2 (en)	2000-03-30
MX202561B (de)	2001-06-21
KR100430538B1 (ko)	2005-01-15
US6030977A (en)	2000-02-29
ES2179327T3 (es)	2003-01-16
MX9808761A (es)	1999-02-28
GB9608771D0 (en)	1996-07-03
HU228649B1 (en)	2013-04-29
CA2252958C (en)	2006-08-01
CN1222054A (zh)	1999-07-07
ATE222455T1 (de)	2002-09-15

Publication	Publication Date	Title
US4146716A (en)	1979-03-27	Thienopyrimidines
PL188823B1 (pl)	2005-04-29	Sól pirymetanilu i zawierająca ją kompozycja grzybobójcza
EP0248086B1 (de)	1993-03-17	Imidazolabkömmlinge, bakterizide, die diese enthalten und herstellungsverfahren
SU969160A3 (ru)	1982-10-23	Способ получени 2-ариламиногексагидропиримидинов или имидазолидинов или их солей или их комплексов с сол ми металлов
US4535087A (en)	1985-08-13	N-Substituted phenoxyacetamide fungicides
US4000138A (en)	1976-12-28	Organic compounds and compositions containing them
CA1174866A (en)	1984-09-25	Plant growth regulating cyano-phenyl-acetamide derivatives
JPS58128380A (ja)	1983-07-30	新規イミダゾ−ル化合物、それらの製造方法及びそれらからなる抗体外寄生生物、駆虫剤
EP0432894A1 (de)	1991-06-19	Fungizide Zusammensetzung
EP0008145B1 (de)	1984-02-01	Verwendung von Penyliminomethylpyridine-Derivate als Fungizide und Pflanzenwachstums-Regulatoren, sie enthaltende Zusmammensetzungen, phenyliminomethylpyridine-Derivate und deren Herstellung
US4199583A (en)	1980-04-22	Antifungal method, formulations and compounds
US4339453A (en)	1982-07-13	Antimicrobial aminopyrimidinium salts
US4189483A (en)	1980-02-19	Pesticidal compounds, compositions and processes
EP0375414B1 (de)	1994-06-15	Guanidin- und Amidin-Verbindungen, deren Herstellung und Verwendung als Fungizide
MXPA98008761A (en)	1999-04-06	Fungicide sales
US4260624A (en)	1981-04-07	Fungicidal 2-substituted-3-oxa-3a lambda4,4-dithia-6-chloro-1,5-diazapentalene
US4230711A (en)	1980-10-28	Fungicidal n-substituted 4,4-dialkyl homophthalimides
AU586175B2 (en)	1989-07-06	Azolyl derivatives of carbocyclic and heterocyclic ketones having fungicidal activity
US3962442A (en)	1976-06-08	Fungicidal compositions containing 2-amino pyrimidines and methods of using the same
US4271306A (en)	1981-06-02	2-Arylthio-4,4-dialkyl-5-methylene-1,3-thiazolines
EP0122410A2 (de)	1984-10-24	Fungizide Isonikotinanilid-acetal-Derivate, Verfahren zu deren Herstellung und diese enthaltende Fungizide
EP4653423A1 (de)	2025-11-26	Pyrazol-5-etherverbindung und herstellungsverfahren dafür und verwendung davon
JPH04178305A (ja)	1992-06-25	ジメチルポリシロキサンエチレンオキサイドプロピレンオキサイドブロックポリマー付加物を含有する殺菌剤組成物
JPH0426681A (ja)	1992-01-29	アルキルアミノピリミジン誘導体、その製造法及び有害生物防除剤
JPH04173704A (ja)	1992-06-22	アルキルジメチルアミノ酢酸ベタインを含有する殺菌剤組成物